A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518418



Internal ID15445711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54461987..54487114hg38UCSC Ensembl
Innerchr15:54754185..54779312hg19UCSC Ensembl
Innerchr15:52541477..52566604hg18UCSC Ensembl
Innerchr15:52541477..52566604hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3825128
hg1925128
hg1825128
hg1725128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n21
Supporting Variantsnssv695853
Samples
Known GenesUNC13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518418
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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